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Volumn 36, Issue 4, 2003, Pages 264-275

Synthetic aspects of stereoselective hydroformylation

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE;

EID: 0037393960     PISSN: 00014842     EISSN: None     Source Type: Journal    
DOI: 10.1021/ar0200596     Document Type: Article
Times cited : (214)

References (53)
  • 1
    • 0000610199 scopus 로고
    • (Chemische Verwertungsgesellschaft, mbH Oberhausen) German Patent DE 849,548, 1938/1952; U.S. Patent 2,317,066, 1943
    • Roelen, O. (Chemische Verwertungsgesellschaft, mbH Oberhausen) German Patent DE 849,548, 1938/1952; U.S. Patent 2,317,066, 1943; Chem. Abstr. 1944, 38, 550.
    • (1944) Chem. Abstr. , vol.38 , pp. 550
    • Roelen, O.1
  • 3
    • 0026418434 scopus 로고
    • The atom economy - A search for synthetic efficiency
    • Trost, B. M. The Atom Economy - A Search for Synthetic Efficiency. Science 1991, 254, 1471-1477; Atom Economy - A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way. Angew. Chem., Int. Ed. Engl. 1995, 34, 259-281.
    • (1991) Science , vol.254 , pp. 1471-1477
    • Trost, B.M.1
  • 4
    • 33750309194 scopus 로고
    • Atom economy - A challenge for organic synthesis: Homogeneous catalysis leads the way
    • Trost, B. M. The Atom Economy - A Search for Synthetic Efficiency. Science 1991, 254, 1471-1477; Atom Economy - A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way. Angew. Chem., Int. Ed. Engl. 1995, 34, 259-281.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 259-281
  • 5
    • 0035157151 scopus 로고    scopus 로고
    • Recent advances on chemo-regio- and stereoselective hydroformylation
    • Breit, B.; Seiche, W. Recent Advances on Chemo-Regio- and Stereoselective Hydroformylation. Synthesis 2001, 1-36.
    • (2001) Synthesis , pp. 1-36
    • Breit, B.1    Seiche, W.2
  • 6
    • 37049124551 scopus 로고
    • Hydroformylation of alkenes by use of rhodium complex catalysts
    • Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
    • (1968) J. Chem. Soc. A , pp. 3133-3142
    • Evans, D.A.1    Osborn, J.A.2    Wilkinson, G.3
  • 7
    • 37049125199 scopus 로고
    • Homogeneous hydroformylation of alkenes with hydridocarbonyltris-(triphenylphosphine)rhodium(I) as catalyst
    • Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
    • (1970) J. Chem. Soc. A , vol.17 , pp. 2753-2764
    • Brown, C.K.1    Wilkinson, G.2
  • 8
    • 0002980921 scopus 로고
    • Homogeneous hydrogenation and hydroformylation of olefins by rhodium triphenylphosphine catalysts
    • Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
    • (1968) Bull. Soc. Chim. Fr. , pp. 5055-5058
    • Wilkinson, G.1
  • 9
    • 37049133322 scopus 로고
    • The preparation and properties of tris(triphenylphosphine)halogeno-rhodium(I) and some reactions thereof including catalytic homogeneous hydrogenation of olefins and acetylenes and their derivatives
    • Evans, D. A.; Osborn, J. A.; Wilkinson, G. Hydroformylation of Alkenes by Use of Rhodium Complex Catalysts. J. Chem. Soc. A 1968, 3133-3142. Brown, C. K.; Wilkinson, G. Homogeneous Hydroformylation of Alkenes with Hydridocarbonyltris-(triphenylphosphine)rhodium(I) as Catalyst. J. Chem. Soc. A 1970, 17, 2753-2764. Wilkinson, G. Homogeneous Hydrogenation and Hydroformylation of Olefins by Rhodium Triphenylphosphine Catalysts. Bull. Soc. Chim. Fr. 1968, 5055-5058. Osborn, J. A.; Jardine, F. H.; Young, J. F.; Wilkinson, G. The Preparation and Properties of Tris(triphenylphosphine)halogeno-rhodium(I) and Some Reactions thereof including Catalytic Homogeneous Hydrogenation of Olefins and Acetylenes and their Derivatives. J. Chem. Soc. A 1966, 1711-1732.
    • (1966) J. Chem. Soc. A , pp. 1711-1732
    • Osborn, J.A.1    Jardine, F.H.2    Young, J.F.3    Wilkinson, G.4
  • 11
    • 85005607967 scopus 로고
    • The natural bite angle of chelating diphosphines
    • Casey, C. P.; Whiteker, G. T. The natural bite angle of chelating diphosphines. Isr. J. Chem. 1990, 30, 299-304.
    • (1990) Isr. J. Chem. , vol.30 , pp. 299-304
    • Casey, C.P.1    Whiteker, G.T.2
  • 12
    • 11944256836 scopus 로고
    • Diphosphines with natural bite angles near 120.degree. Increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation
    • Casey, C. P.; Whiteker, G. T.; Melville, M. G.; Petrovich, L. M.; Gavey, J. A.; Powell, D. R. Diphosphines with natural bite angles near 120.degree. Increase selectivity for n-aldehyde formation in rhodium-catalyzed hydroformylation. J. Am. Chem. Soc. 1992, 114, 5535-5543.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5535-5543
    • Casey, C.P.1    Whiteker, G.T.2    Melville, M.G.3    Petrovich, L.M.4    Gavey, J.A.5    Powell, D.R.6
  • 13
    • 84921186420 scopus 로고
    • (UCC) U.S. Patent 4,769,498, 1988
    • Billig, E.; Abatjoglou, A. G.; Bryant, D. R. (UCC) U.S. Patent 4,769,498, 1988; Chem. Abstr. 1989, 111, 117 287. Cunny, G. D.; Buchwald, S. L. Practical, high-yield, regioselective, rhodiumcatalyzed hydroformylation of functionalized.alpha.-olefins. J. Am. Chem. Soc. 1993, 115, 2066-2068.
    • (1989) Chem. Abstr. , vol.111 , pp. 117-287
    • Billig, E.1    Abatjoglou, A.G.2    Bryant, D.R.3
  • 14
    • 84921186420 scopus 로고
    • Practical, high-yield, regioselective, rhodiumcatalyzed hydroformylation of functionalized.alpha.-olefins
    • Billig, E.; Abatjoglou, A. G.; Bryant, D. R. (UCC) U.S. Patent 4,769,498, 1988; Chem. Abstr. 1989, 111, 117 287. Cunny, G. D.; Buchwald, S. L. Practical, high-yield, regioselective, rhodiumcatalyzed hydroformylation of functionalized.alpha.-olefins. J. Am. Chem. Soc. 1993, 115, 2066-2068.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 2066-2068
    • Cunny, G.D.1    Buchwald, S.L.2
  • 15
    • 0001029926 scopus 로고
    • New diphosphine ligands based on heterocyclic aromatics inducing very high regioselectivity in rhodium-catalyzed hydroformylation: Effect of the bite angle
    • Kranenburg, M.; van der Burgt, Y. E. M.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Goubitz, K.; Fraanje, J. New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle. Organometallics 1995, 14, 3081-3089. Kamer C. J. P.; van Leeuwen, P. W. N. M.; Reek, J. N. H. Wide Bite Angle Diphosphines: Xantphos Ligands in Transition Metal Complexes and Catalysis. Acc. Chem. Res. 2001, 34, 895-904.
    • (1995) Organometallics , vol.14 , pp. 3081-3089
    • Kranenburg, M.1    Van der Burgt, Y.E.M.2    Kamer, P.C.J.3    Van Leeuwen, P.W.N.M.4    Goubitz, K.5    Fraanje, J.6
  • 16
    • 0035200787 scopus 로고    scopus 로고
    • Wide bite angle diphosphines: Xantphos ligands in transition metal complexes and catalysis
    • Kranenburg, M.; van der Burgt, Y. E. M.; Kamer, P. C. J.; van Leeuwen, P. W. N. M.; Goubitz, K.; Fraanje, J. New Diphosphine Ligands Based on Heterocyclic Aromatics Inducing Very High Regioselectivity in Rhodium-Catalyzed Hydroformylation: Effect of the Bite Angle. Organometallics 1995, 14, 3081-3089. Kamer C. J. P.; van Leeuwen, P. W. N. M.; Reek, J. N. H. Wide Bite Angle Diphosphines: Xantphos Ligands in Transition Metal Complexes and Catalysis. Acc. Chem. Res. 2001, 34, 895-904.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 895-904
    • Kamer, C.J.P.1    Van Leeuwen, P.W.N.M.2    Reek, J.N.H.3
  • 18
    • 85013461641 scopus 로고    scopus 로고
    • Highly enantioselective hydroformylation of olefins catalyzed by new phosphine phosphite-rhodium(I) complexes
    • Sakai, N.; Mano, S.; Nozaki, K.; Takaya, H. Highly enantioselective hydroformylation of olefins catalyzed by new phosphine phosphite-rhodium(I) complexes. J. Am. Chem. Soc. 1993, 115, 7033. Nozaki, K.; Ojima, I. Asymmetric Carbonylations. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley-VCH: New York, 2000; Chapter 7.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 7033
    • Sakai, N.1    Mano, S.2    Nozaki, K.3    Takaya, H.4
  • 19
    • 85013461641 scopus 로고    scopus 로고
    • Asymmetric carbonylations
    • Ojima, I., Ed.; Wiley-VCH: New York; Chapter 7
    • Sakai, N.; Mano, S.; Nozaki, K.; Takaya, H. Highly enantioselective hydroformylation of olefins catalyzed by new phosphine phosphite-rhodium(I) complexes. J. Am. Chem. Soc. 1993, 115, 7033. Nozaki, K.; Ojima, I. Asymmetric Carbonylations. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley-VCH: New York, 2000; Chapter 7.
    • (2000) Catalytic Asymmetric Synthesis
    • Nozaki, K.1    Ojima, I.2
  • 20
    • 0001475165 scopus 로고
    • Synthese von zwischenprodukten durch rhodiumkatalysierte hydroformylierung
    • Siegel, H.; Himmele W. Synthese von Zwischenprodukten durch rhodiumkatalysierte Hydroformylierung. Angew. Chem. 1980, 92, 182-187; Synthesis of intermediate products by rhodiumcatalyzed hydroformylation. Angew. Chem., Int. Ed. Engl. 1980, 19, 178-183.
    • (1980) Angew. Chem. , vol.92 , pp. 182-187
    • Siegel, H.1    Himmele, W.2
  • 21
    • 84985560802 scopus 로고
    • Synthesis of intermediate products by rhodiumcatalyzed hydroformylation
    • Siegel, H.; Himmele W. Synthese von Zwischenprodukten durch rhodiumkatalysierte Hydroformylierung. Angew. Chem. 1980, 92, 182-187; Synthesis of intermediate products by rhodiumcatalyzed hydroformylation. Angew. Chem., Int. Ed. Engl. 1980, 19, 178-183.
    • (1980) Angew. Chem., Int. Ed. Engl. , vol.19 , pp. 178-183
  • 22
    • 0035898365 scopus 로고    scopus 로고
    • Phosphabenzenes as monodentate π-acceptor ligands for rhodium-catalyzed hydroformylation
    • Breit, B.; Winde, R.; Mackewitz, T.; Paciello, R.; Harms, K. Phosphabenzenes as Monodentate π-Acceptor Ligands for Rhodium-Catalyzed Hydroformylation. Chem. Eur. J. 2001, 7, 3106-3121.
    • (2001) Chem. Eur. J. , vol.7 , pp. 3106-3121
    • Breit, B.1    Winde, R.2    Mackewitz, T.3    Paciello, R.4    Harms, K.5
  • 23
    • 0025113889 scopus 로고
    • Total synthesis of (+)-phyllanthocin. Introduction of intramolecular hydroformylation for complex molecule functionalization
    • Burke, S. D.; Cobb, J. E.; Takeuchi, K. Total synthesis of (+)-phyllanthocin. Introduction of intramolecular hydroformylation for complex molecule functionalization. J. Org. Chem. 1990, 55, 2138-2151.
    • (1990) J. Org. Chem. , vol.55 , pp. 2138-2151
    • Burke, S.D.1    Cobb, J.E.2    Takeuchi, K.3
  • 24
    • 84970564851 scopus 로고
    • The stereochemistry of organometallic compounds. XXXVIII* regio- and stereo-control in the rhodium-catalysed hydroformylation of some alkenyl phosphites
    • Jackson, W. R.; Moffat, M. R.; Perlmutter, P.; Tasdelen, E. E. The Stereochemistry of Organometallic Compounds. XXXVIII* Regio- and Stereo-control in the Rhodium-Catalysed Hydroformylation of Some Alkenyl Phosphites. Aust. J. Chem. 1992, 45, 823-834.
    • (1992) Aust. J. Chem. , vol.45 , pp. 823-834
    • Jackson, W.R.1    Moffat, M.R.2    Perlmutter, P.3    Tasdelen, E.E.4
  • 25
    • 0030590401 scopus 로고    scopus 로고
    • Diastereoselective hydroformylation of certain protected allylic alcohols
    • Doi, T.; Komatsu, H.; Yamamoto, K. Diastereoselective Hydroformylation of Certain Protected Allylic Alcohols. Tetrahedron Lett. 1996, 37, 6877-6880.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 6877-6880
    • Doi, T.1    Komatsu, H.2    Yamamoto, K.3
  • 26
    • 0000458209 scopus 로고
    • Substrate-directable reactions
    • Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Substrate-Directable Reactions. Chem. Rev. 1993, 93, 1307-1370. Brown, J. M. Intramolekular gesteuerte katalytische Hydrierungen in homogener Phase. Angew. Chem. 1987, 99, 169-182; Directed Homogeneous Hydrogenation. Angew. Chem., Int. Ed. Engl. 1987, 26, 190-203.
    • (1993) Chem. Rev. , vol.93 , pp. 1307-1370
    • Hoveyda, A.H.1    Evans, D.A.2    Fu, G.C.3
  • 27
    • 0000458209 scopus 로고
    • Intramolekular gesteuerte katalytische hydrierungen in homogener phase
    • Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Substrate-Directable Reactions. Chem. Rev. 1993, 93, 1307-1370. Brown, J. M. Intramolekular gesteuerte katalytische Hydrierungen in homogener Phase. Angew. Chem. 1987, 99, 169-182; Directed Homogeneous Hydrogenation. Angew. Chem., Int. Ed. Engl. 1987, 26, 190-203.
    • (1987) Angew. Chem. , vol.99 , pp. 169-182
    • Brown, J.M.1
  • 28
    • 84985560333 scopus 로고
    • Directed homogeneous hydrogenation
    • Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Substrate-Directable Reactions. Chem. Rev. 1993, 93, 1307-1370. Brown, J. M. Intramolekular gesteuerte katalytische Hydrierungen in homogener Phase. Angew. Chem. 1987, 99, 169-182; Directed Homogeneous Hydrogenation. Angew. Chem., Int. Ed. Engl. 1987, 26, 190-203.
    • (1987) Angew. Chem., Int. Ed. Engl. , vol.26 , pp. 190-203
  • 29
    • 0000680768 scopus 로고    scopus 로고
    • Diastereoselective hydroformylation of methallylic alcohols
    • Breit, B. Diastereoselective Hydroformylation of Methallylic Alcohols. Angew. Chem. 1996, 108, 3021-3023; Angew. Chem., Int. Ed. Engl. 1996, 35, 2835-2837.
    • (1996) Angew. Chem. , vol.108 , pp. 3021-3023
    • Breit, B.1
  • 30
    • 0030484567 scopus 로고    scopus 로고
    • Breit, B. Diastereoselective Hydroformylation of Methallylic Alcohols. Angew. Chem. 1996, 108, 3021-3023; Angew. Chem., Int. Ed. Engl. 1996, 35, 2835-2837.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 2835-2837
  • 31
    • 0003719460 scopus 로고    scopus 로고
    • Substrate-directed diastereoselective hydroformylation of methallylic alcohols-development of an efficient catalyst-directing group for rhodium-catalyzed hydroformylation
    • Breit, B. Substrate-Directed Diastereoselective Hydroformylation of Methallylic Alcohols-Development of an Efficient Catalyst-Directing Group for Rhodium-Catalyzed Hydroformylation. Liebigs Ann./Recueil 1997, 1841-1851.
    • (1997) Liebigs Ann./Recueil , pp. 1841-1851
    • Breit, B.1
  • 32
    • 0002177913 scopus 로고    scopus 로고
    • Asymmetric allylic alkylation
    • Ojima, I., Ed.; Wiley-VCH: New York, Chapter 8E
    • Ortho-diphenylbenzoic acid is also an integral part of the Trost type ligands for the enantioselective palladium-catalyzed allylic substitution, see: Trost, B. M.; Chulbom L. Asymmetric Allylic Alkylation. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley-VCH: New York, 2000, Chapter 8E.
    • (2000) Catalytic Asymmetric Synthesis
    • Trost, B.M.1    Chulbom, L.2
  • 33
    • 0344640634 scopus 로고    scopus 로고
    • Unpublished results from these laboratories
    • Breit, B.; Zahn, S. K. Unpublished results from these laboratories, 2001.
    • (2001)
    • Breit, B.1    Zahn, S.K.2
  • 34
    • 0037455326 scopus 로고    scopus 로고
    • Diastereoselective hydroformylation of 2-substituted allylic-o-DPPB-esters - On the origin of 1,2-asymmetric induction
    • in press
    • Breit, B.; Heckmann, G.; Zahn, S. K. Diastereoselective Hydroformylation of 2-Substituted Allylic-o-DPPB-Esters - On the Origin of 1,2-Asymmetric Induction. Chem. Eur. J. 2003, 9, in press.
    • (2003) Chem. Eur. J. , vol.9
    • Breit, B.1    Heckmann, G.2    Zahn, S.K.3
  • 35
    • 0032820019 scopus 로고    scopus 로고
    • Substrate-directed diastereoselective hydroformylation: Key step for the assembly of polypropionate subunits
    • Breit, B.; Dauber, M.; Harms, K. Substrate-Directed Diastereoselective Hydroformylation: Key step for the Assembly of Polypropionate Subunits, Chem. Eur. J. 1999, 5, 2819-2827.
    • (1999) Chem. Eur. J. , vol.5 , pp. 2819-2827
    • Breit, B.1    Dauber, M.2    Harms, K.3
  • 36
    • 84985611207 scopus 로고
    • Stereoselective syntheses of building blocks with three consecutive stereogenic centers: Important precursors of polyketide natural products
    • Hoffmann, R. W. Stereoselective Syntheses of Building Blocks with Three Consecutive Stereogenic Centers: Important Precursors of Polyketide Natural Products. Angew. Chem., Int. Ed. Engl. 1987, 26, 489-503.
    • (1987) Angew. Chem., Int. Ed. Engl. , vol.26 , pp. 489-503
    • Hoffmann, R.W.1
  • 37
    • 0035854318 scopus 로고    scopus 로고
    • Stereoselective hydroformylation: Key step for the assembly of polypropionate subunits
    • Breit, B.; Zahn, S. K. Stereoselective Hydroformylation: Key Step for the Assembly of Polypropionate Subunits. J. Org. Chem. 2001, 66, 4870-4877.
    • (2001) J. Org. Chem. , vol.66 , pp. 4870-4877
    • Breit, B.1    Zahn, S.K.2
  • 38
    • 0032473817 scopus 로고    scopus 로고
    • Diastereoselective hydroformylation of acyclic olefins: Efficient construction of an all-anti stereotriade building block for polyketide synthesis
    • Breit, B.; Zahn, S. K. Diastereoselective hydroformylation of acyclic olefins: efficient construction of an all-anti stereotriade building block for polyketide synthesis. Tetrahedron Lett. 1998, 39, 1901-1904.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 1901-1904
    • Breit, B.1    Zahn, S.K.2
  • 39
    • 0001449130 scopus 로고    scopus 로고
    • Highly stereoselective hydroformylation of olefins possessing chiral sugartemplates
    • Takahashi, T.; Ebata, S.; Yamada, H. Highly stereoselective hydroformylation of olefins possessing chiral sugartemplates. Synlett. 1998, 381-382.
    • (1998) Synlett , pp. 381-382
    • Takahashi, T.1    Ebata, S.2    Yamada, H.3
  • 40
    • 0035929981 scopus 로고    scopus 로고
    • Highly regioselective and diastereoselective directed hydroformylation of allylic ethers: A new approach to propionate aldol synthesis
    • Krauss, I. J.; Wang, C. C.-Y.; Leighton, J. L. Highly Regioselective and Diastereoselective Directed Hydroformylation of Allylic Ethers: A New Approach to Propionate Aldol Synthesis. J. Am. Chem. Soc. 2001, 123, 11514-11515.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 11514-11515
    • Krauss, I.J.1    Wang, C.C.-Y.2    Leighton, J.L.3
  • 41
    • 0000287486 scopus 로고    scopus 로고
    • Substrate directed diastereoselective hydroformylation of acyclic homomethallylic alcohols
    • Breit, B. Substrate directed diastereoselective hydroformylation of acyclic homomethallylic alcohols. J. Chem. Soc., Chem. Commun. 1997, 591-592.
    • (1997) J. Chem. Soc., Chem. Commun. , pp. 591-592
    • Breit, B.1
  • 42
    • 2742537764 scopus 로고    scopus 로고
    • 1,3-Asymmetric induction in stereoselective rhodium-catalyzed hydroformylation of homomethallylic alcohols
    • Breit, B. 1,3-Asymmetric Induction in Stereoselective Rhodium-Catalyzed Hydroformylation of Homomethallylic Alcohols. Eur. J. Org. Chem. 1998, 3, 1123-1134.
    • (1998) Eur. J. Org. Chem. , vol.3 , pp. 1123-1134
    • Breit, B.1
  • 43
    • 0030726113 scopus 로고    scopus 로고
    • Highly diastereoselective rhodium-catalyzed hydroformylation of enol ethers: A carbonylation-based approach to catalytic aldol synthesis
    • Leighton, J. L.; O'Neil, D. N. Highly Diastereoselective Rhodium-Catalyzed Hydroformylation of Enol Ethers: A Carbonylation-Based Approach to Catalytic Aldol Synthesis. J. Am. Chem. Soc. 1997, 119, 11118-11119.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11118-11119
    • Leighton, J.L.1    O'Neil, D.N.2
  • 45
    • 84975921727 scopus 로고    scopus 로고
    • (IG Farben), DRP, a. I. 74,946, 1943
    • Reppe, W. (IG Farben), DRP, a. I. 74,946, 1943; Reppe, W.; Kindler, W. Synthese mit Metallcarbonylwasserstoffen. Liebigs Ann. Chem. 1953, 582, 133-161.
    • Reppe, W.1
  • 46
    • 84975921727 scopus 로고    scopus 로고
    • Synthese mit metallcarbonylwasserstoffen
    • Reppe, W. (IG Farben), DRP, a. I. 74,946, 1943; Reppe, W.; Kindler, W. Synthese mit Metallcarbonylwasserstoffen. Liebigs Ann. Chem. 1953, 582, 133-161.
    • (1953) Liebigs Ann. Chem. , vol.582 , pp. 133-161
    • Reppe, W.1    Kindler, W.2
  • 47
    • 0032537696 scopus 로고    scopus 로고
    • Substrate-directed diastereoselective hydroaminomethylation of methallylic alcohols
    • B. Breit Substrate-Directed Diastereoselective Hydroaminomethylation of Methallylic Alcohols. Tetrahedron Lett. 1998, 39, 5163-5166.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5163-5166
    • Breit, B.1
  • 48
    • 0034678104 scopus 로고    scopus 로고
    • Tandem hydroformylation/aldol addition of silyl enol ethers bearing remote olefinic functionalities
    • Hollmann, C.; Eilbracht, P. Tandem Hydroformylation/Aldol Addition of Silyl Enol Ethers Bearing Remote Olefinic Functionalities. Tetrahedron 2000, 56, 1685-1692.
    • (2000) Tetrahedron , vol.56 , pp. 1685-1692
    • Hollmann, C.1    Eilbracht, P.2
  • 49
    • 0342614249 scopus 로고    scopus 로고
    • Domino-hydroformylation-allylboration-hydroformylation for the synthesis of trans-2-alkylpiperidin-3-ols
    • Hoffmann, R. W.; Brückner, D.; Gerusz, V. J. Domino-hydroformylation-allylboration-hydroformylation for the synthesis of trans-2-alkylpiperidin-3-ols. Heterocycles 2000, 52, 121-124.
    • (2000) Heterocycles , vol.52 , pp. 121-124
    • Hoffmann, R.W.1    Brückner, D.2    Gerusz, V.J.3
  • 50
    • 0001615148 scopus 로고    scopus 로고
    • Domino hydroformylation wittig reactions
    • Breit, B.; Zahn, S. K. Domino Hydroformylation Wittig Reactions. Angew. Chem. 1999, 111, 1022-1024; Angew. Chem., Int. Ed. Engl. 1999, 38, 969-971.
    • (1999) Angew. Chem. , vol.111 , pp. 1022-1024
    • Breit, B.1    Zahn, S.K.2
  • 51
    • 0033119121 scopus 로고    scopus 로고
    • Breit, B.; Zahn, S. K. Domino Hydroformylation Wittig Reactions. Angew. Chem. 1999, 111, 1022-1024; Angew. Chem., Int. Ed. Engl. 1999, 38, 969-971.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 969-971
  • 52
    • 0000020751 scopus 로고    scopus 로고
    • Domino hydroformylation-knoevenagel-hydrogenation reactions
    • Breit, B.; Zahn, S. K. Domino Hydroformylation-Knoevenagel-Hydrogenation Reactions. Angew. Chem. 2001, 113, 1964-1967; Angew. Chem., Int. Ed. 2001, 40, 1910-1913.
    • (2001) Angew. Chem. , vol.113 , pp. 1964-1967
    • Breit, B.1    Zahn, S.K.2
  • 53
    • 0035906868 scopus 로고    scopus 로고
    • Breit, B.; Zahn, S. K. Domino Hydroformylation-Knoevenagel-Hydrogenation Reactions. Angew. Chem. 2001, 113, 1964-1967; Angew. Chem., Int. Ed. 2001, 40, 1910-1913.
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 1910-1913


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